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ERCC1 as a Predictive Marker for FOLFOX Chemotherapy in an Adjuvant Setting.
Kim, Chee Young; Seo, Sang Hyuk; An, Min Sung; Kim, Kwang Hee; Bae, Ki Beom; Hwang, Jin Won; Kim, Ji Hyun; Kim, Bo Mi; Kang, Mi Seon; Oh, Min Kyung; Hong, Kwan Hee.
Afiliação
  • Kim CY; Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Seo SH; Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • An MS; Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Kim KH; Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Bae KB; Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Hwang JW; Department of Internal Medicine, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Kim JH; Department of Internal Medicine, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Kim BM; Department of Pathology, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Kang MS; Department of Pathology, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Oh MK; Clinical Trial Center in Pharmacology, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • Hong KH; Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
Ann Coloproctol ; 31(3): 92-7, 2015 Jun.
Article em En | MEDLINE | ID: mdl-26161376
ABSTRACT

PURPOSE:

The purpose of this study was to identify the excision repair cross-complementation group 1 (ERCC1) as a predictive marker for FOLFOX adjuvant chemotherapy in stages II and III colon cancer patients.

METHODS:

A total of 166 high risk stages II and III colon cancer patients were retrospectively enrolled in this study, and data were collected prospectively. They underwent a curative resection followed by FOLFOX4 adjuvant chemotherapy. We analyzed ERCC1 expression in the primary colon tumor by using immunohistochemical staining. The oncological outcomes included the 5-year disease-free survival (DFS) rate. The DFS was analyzed by using the Kaplan-Meier method with the log-rank test. A Cox proportional hazard model was used for the prognostic analysis.

RESULTS:

ERCC1-positive expression was statistically significant in the older patients (P = 0.032). In the multivariate analysis, the prognostic factors for DFS were female sex (P = 0.016), N stage (P = 0.009), and postoperative carcinoembryonic antigen level (P = 0.001), but ERCC1 expression was not a statistically significant prognostic factor for DFS in the univariate analysis (P = 0.397). The 5-year DFS rate was not significantly associated with the ERCC1 expression in all patients (P = 0.396) or with stage III disease (P = 0.582).

CONCLUSION:

We found that ERCC1 expression was not significantly correlated with the 5-year DFS as reflected by the oncologic outcomes in patients with high-risk stages II and III colon cancer treated with FOLFOX adjuvant chemotherapy.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Ann Coloproctol Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Ann Coloproctol Ano de publicação: 2015 Tipo de documento: Article